| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5274760 | Tetrahedron Letters | 2011 | 4 Pages |
Abstract
Reaction of cyclic diazoamides with furan systems using rhodium(II) acetate as a catalyst afforded a variety of (3Z)-3-[(2E)-4-oxopent-2-en-1-ylidene]indol-2-ones in a regio- and diastereo-selective manner. The diastereoselectivity was based on the flow rate of cyclic diazoamides. The representative products were characterized by single-crystal X-ray analyses.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Sengodagounder Muthusamy, Datshanamoorthy Azhagan,